Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
  • B01J20/26—Synthetic macromolecular compounds
  • B01J20/261—Synthetic macromolecular compounds obtained by reactions only involving carbon to carbon unsaturated bonds
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
  • B01J20/26—Synthetic macromolecular compounds
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D53/00—Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
  • B01D53/26—Drying gases or vapours
  • B01D53/28—Selection of materials for use as drying agents
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
  • B01J20/30—Processes for preparing, regenerating, or reactivating
  • B01J20/3042—Use of binding agents; addition of materials ameliorating the mechanical properties of the produced sorbent
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F8/00—Chemical modification by after-treatment
  • C08F8/12—Hydrolysis
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
  • C08F2800/00—Copolymer characterised by the proportions of the comonomers expressed
  • C08F2800/20—Copolymer characterised by the proportions of the comonomers expressed as weight or mass percentages
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S526/00—Synthetic resins or natural rubbers -- part of the class 520 series
  • Y10S526/909—Polymerization characterized by particle size of product

Definitions

• the present invention relates to moisture adsorptive and desorptive fine particles which perform moisture adsorption and desorption reversibly and withstand repeated use.
• a conventional way of removing moisture from air resorts to moisture absorbents such as lithium chloride, calcium chloride, magnesium chloride, and phosphorus pentoxide.
• moisture absorbents such as lithium chloride, calcium chloride, magnesium chloride, and phosphorus pentoxide.
• Other moisture absorbents such as silica gel, zeolite, sodium sulfate, activated alumina, and activated carbon suffer the disadvantage of being limited in the amount of moisture absorption, being slow in the rate of moisture absorption, and requiring high temperature for their regeneration. This prevents them from being put to practical use.
• This moisture absorbent absorbs a large amount of moisture, can be regenerated easily by drying, and has such a small particle diameter that it does not impair the appearance and physical properties of the base material when used as an additive.
• the above-mentioned object of the present invention can be achieved by high moisture adsorptive and desorptive fine particles characterized in that said particles are of crosslinked acrylonitrile polymer and are 1.0-15.0% by weight of the increase in nitrogen content due to crosslinking by hydrazine, there being introduced salt type carboxyl groups in an amount of 1.0 mmol/g or more into a part of the remaining nitrile groups, and the particle diameter of said fine particles being 10 ⁇ m or less.
• the above-mentioned object of the present invention can also be achieved by a process for producing high moisture adsorptive and desorptive fine particles characterized in that an emulsion of an acrylonitrile polymer is subjected to the treatment with hydrazine to introduce crosslinking bond into the fine particles so that the increase in the nitrogen content is 1.0-15.0% by weight, and then subjected to hydrolysis so that there are introduced carboxyl groups into 1.0 mmol/g or more of the remaining nitrile groups and amide groups are introduced into all of the remaining nitrile groups, said carboxyl groups being in the form of salt type.
• the product according to the present invention is in the form of fine particles of crosslinked acrylonitrile polymer. It is produced from fine particles of acrylonitrile polymer containing more than 40 wt %, preferably more than 50 wt %, of acrylonitrile (AN for short hereinafter).
• the AN polymer may be either a homopolymer or a copolymer with a comonomer.
• Examples of the comonomer include vinyl halide and vinylidene halide; (meth) acrylic ester; sulfonic acid-containing monomer and salt thereof (such as methallylsulfonic acid and p-styrenesulfonic acid and the like); carboxylic acid-containing monomer and salt thereof (such as (meth) acrylic acid and itaconic acid and the like); and acrylamide, styrene, and vinyl acetate and the like.
• the AN polymer fine particles as the starting material can be prepared typically by the process disclosed in Japanese Patent Publication No. 2207/1980. The present invention is not limited to this process.
• the method of introducing hydrazine crosslinks (crosslinking) into the AN polymer fine particles is not specifically limited so long as it is capable of increasing the nitrogen content by 1.0-15.0 wt %.
• An industrially favorable method is treatment at 50°-120° C. for 0.5-5 hours in the form of emulsion containing 6-80% of hydrazine.
• Increase in nitrogen content means the difference between the nitrogen content (in wt % based on fine particles) in AN polymer fine particles as the starting material and the nitrogen content (in wt % based on fine particles) in hydrazine-crosslinked AN polymer fine particles.
• the fine particles will dissolve in water in the subsequent step of hydrolysis which is intended to introduce carboxyl groups, and hence the object of the present invention is not achieved. If the increase in nitrogen content exceeds the upper limit specified above, the fine particles do not accept more than 1.0 mmol/g of carboxyl groups in the subsequent step, and hence the object of the present invention is not achieved.
• the condition under which the nitrogen content increases by 1.0-15.0 wt % will vary depending on the reaction temperature and time and the concentrations of reactants which may be determined easily by experiment. Examples of the hydrazine include hydrazine hydrate, hydrazine sulfate, hydrazine hydrochloride, hydrazine nitrate, and hydrazine hydrobromide and the like.
• nitrile groups remaining intact after crosslinking by hydrazine are substantially eliminated by hydrolysis in such a manner that more than 1.0 mmol/g of carboxyl groups in salt form are introduced into nitrile groups and amide groups are introduced into the rest of nitrile groups.
• This process is accomplished by heat treatment in the presence of an alkaline aqueous solution of alkali metal hydroxide or ammonia or a mineral acid such as nitric acid, sulfuric acid, and hydrochloric acid and the like.
• the amount of carboxyl groups in salt form should be more than 1.0 mmol/g.
• This condition may be easily determined by experiment on the relation between the amount of carboxyl groups in salt form and the reaction factors (such as temperature, concentration, and time). Incidentally, it is also possible to carry out hydrolysis simultaneously with the introduction of crosslinks. In the case where an acid is used for hydrolysis, it is necessary to convert the carboxyl groups into those of salt form.
• Salts of carboxyl groups are formed from cationic ion of alkali metals (such as Li, Na, and K and the like), alkaline earth metals (such as Be, Mg, Ca, and Ba and the like), other metals (such as Cu, Zn, Al, Mn, Ag, Fe, Co., and Ni and the like), NH 4 , and organic (such as amine and the like). If the amount of carboxyl groups in salt form is less than the lower limit specified above, the resulting product does not exhibit the desired performance. More than one salt may be used.
• the fine particles should have a particle diameter smaller than 10 ⁇ m.
• the way of achieving this object is not specifically limited. A typical example is disclosed in Japanese Patent Publication No. 2207/1980. A particle diameter greater than 10 ⁇ m leads to a slow rate of moisture absorption. Such fine particles impair the appearance and physical properties of the base material and easily drop off from the base material when used as an additive.
• the fine particles of the present invention have the high moisture adsorptive and desorptive properties.
• a probable reason is as follows: The fact that the fine, particles contain substantially no nitrile groups although they are prepared from AN polymer suggests that side chains attached to polymer chains have the crosslink structure containing nitrogen which is formed by reaction with hydrazine and the carboxyl groups in salt form which are formed by hydrolysis of nitrile groups.
• the crosslinking structure also contributes to moisture absorption judging from the fact that the carboxyl groups in salt form are not enough in quantity for high moisture absorption although they are capable of absorbing and releasing moisture.
• the fine particles after moisture absorption are not sticky suggests a high degree of crosslinking.
• the amount (mmol/g) of carboxyl groups in salt form and the moisture absorption were measured according to the following procedure.
• Amount of carboxyl groups (0.1 ⁇ Y)/X where X is the amount (g) of sample, and Y is the volume (cc) of NaOH solution which was consumed by carboxyl groups.
• W1 is the weight of the dried sample
• W2 is the weight of the conditioned sample
• a 2-liter autoclave was charged with 490 parts of acrylonitrile, 16 parts of sodium p-styrenesulfonate, and 1181 parts of water.
• Di-tert-butylperoxide (as a polymerization initiator) was added in an amount of 0.5% for the total amount of monomer.
• polymerization was carried out with stirring at 150° C. for 23 minutes. After the completion of reaction, stirring was continued until the reaction product was cooled to about 90° C. There was obtained an aqueous dispersion of fine particles (I) having an average particle diameter of 0.2 ⁇ m (measured by a light scattering photometer).
• Fine particles No. 1 obtained in Example 1 were processed so as to convert the carboxyl groups into H form.
• the aqueous dispersion (30 g) was immersed in 1 liter of 5% aqueous solution of salt shown in Table 2 at 40° C. for 5 hours. Subsequently, it was poured into a cellulose tube and placed in running water for one week for dialysis and desalting. There were obtained aqueous dispersions of fine particles Nos. 13 to 16. These samples were tested for characteristic properties. The results are shown in Table 2.
• Example 2 One gram of fine particles No. 1 obtained in Example 1 was allowed to stand in a humidistat (90% humidity) for 24 hours. It was then allowed to stand in a humidistat (40% humidity) for 1 hour. This procedure was repeated twice. The fine particles were tested for moisture adsorption and desorption performance. The results are shown in Table 3.
• Example 2 The same procedure as in Example 1 was repeated except that the amount of acrylonitrile was changed from 490 parts to 450 parts and 40 parts of methyl acrylate was used. There was obtained an aqueous dispersion of fine particles (II). It was treated in the same manner as in Example 1.
• the resulting fine particles had an average particle diameter of 0.2 ⁇ m (measured by a light scattering photometer) and an increase in nitrogen content by 3.4%, with the amount of carboxyl groups in salt form being 4.5 mmol/g.
• the moisture absorption of this sample was 44% at 65% RH.
• Aqueous dispersions were prepared from samples of fine particles differing in particle diameter. (The fine particles have a moisture absorption of 43-46% at 65% RH.) Each aqueous dispersion was mixed with Desmolac 4125 (a product of Sumitomo Bayer Urethane Co., Ltd.) such that the ratio of solids in the resulting mixture was 15/85. The mixture was made into film by wet process. There were obtained film samples Nos. 1 to 6. The film samples were tested for tensile strength. The results are shown in Table 4. For comparison, a film sample No. 7 was prepared which is not incorporated with the fine particles. Its test results are also shown in Table 4.
• the significant feature of the present invention is that high moisture adsorptive and desorptive fine particles having an extremely small particle diameter can be produced in an industrially favorable manner.
• the high moisture adsorptive and desorptive fine particles in this invention do not become sticky after moisture absorption because of the high degree of crosslinking among molecules.
• they can be regenerated easily by drying and used repeatedly. They have such a small particle diameter that they can be added to any material without adverse effect on its physical properties and appearance. Therefore, they will find use in various fields where moisture adsorption and desorption are required.

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• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Chemistry (AREA)
• Analytical Chemistry (AREA)
• General Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Polymers & Plastics (AREA)
• Engineering & Computer Science (AREA)
• Oil, Petroleum & Natural Gas (AREA)
• Solid-Sorbent Or Filter-Aiding Compositions (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

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• 1995
  • 1995-11-02 DE DE69514489T patent/DE69514489T2/de not_active Expired - Lifetime
  • 1995-11-02 EP EP95307835A patent/EP0716882B1/fr not_active Expired - Lifetime
  • 1995-11-20 KR KR1019950042178A patent/KR100338426B1/ko not_active IP Right Cessation
  • 1995-12-08 TW TW084113099A patent/TW320640B/zh not_active IP Right Cessation
• 1997
  • 1997-01-23 US US08/787,878 patent/US5691421A/en not_active Expired - Lifetime

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